FDA Medical Device Recalls (openFDA)
Microbiologics Inc: KWIK-STIK" plus: Clostridium perfringens
- Recall number
- Z-1125-2022
- Recalling firm
- Microbiologics Inc
- Product
- KWIK-STIK" plus: Clostridium perfringens
- Status
- Terminated
- Initiated
- 2022-05-06
- Posted
- not on file
- Terminated
- 2024-01-16
- Reason
- Labeling error.
- Root cause
- Labeling mix-ups
- Action
- The firm issued a recall notification to the consignees beginning on 05/06/2022 via email. The letter informs the consignee to inspect inventory, review lab procedures, use or discard affected product depending on lab procedures, and complete the response form.
- Quantity
- 8 units
- Distribution
- Distributed US Nationwide to IA, TN and internationally to Mexico, Colombia, France, South Africa, United Kingdom.
- Lot, serial or model codes
- catalog number: 0801P; lot number: 801-44-4; expiration date: 05/31/2023; UDI: 20845357019374
- 510(k) numbers
- ["K861022"]
- PMA numbers
- not on file
- Product code
- JTR
- Firm FEI
- 2150138
- Firm city
- Saint Cloud
- Firm state
- MN
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28